Canonical Allele Identifier: CA2001379849
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903436T= , CM000673.2:g.113903436T= GRCh38
NC_000011.9:g.113774158T= , CM000673.1:g.113774158T= GRCh37
NC_000011.8:g.113279368T= NCBI36
NG_011483.1:g.3570T=

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4353T= XP_011541366.1:n.12+4353T=
XM_024448767.1:c.-243+4353T= XP_024304535.1:n.-243+4353T=